LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING— 510(k) K980827

Name: FDA 510(k) clearance K980827
Creator: U.S. Food and Drug Administration
Published: 1998-05-04

Substantially Equivalent

Tucker & Associates

FDA 510(k) clearance K980827 for LATEX FINGER COT, POWDER-FREE, WITH PROTEIN LABELING, Substantially Equivalent on 1998-05-04. Applicant: Tucker & Associates. Device class: 1.

Clearance details

Applicant: Tucker & Associates
Product code: Code LZB
Device class: Class 1
Regulation: 21 CFR 880.6250
Advisory panel: General Hospital
Date received: 1998-03-03
Decision date: 1998-05-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sparks, NV, US

Download summary PDF View on FDA.gov ↗

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